A cutting edge Medical Device company specializing in Orthopedics.
Be in charge of regulatory affairs submission.
Apply, acquire, and sustain Japanese government approval.
Attend lectures and seminars related to regulations.
Respond to PMDA notices.
Formulate documents for reimbursement.
【WHY YOU SHOULD APPLY】
Be a part of a global medical device company.
Work with industry leaders and global businesses.
Generous earning potential.
1-3 year experience in Medical Device Regulatory Affairs; document submissions.
Must have at least conversational English and fluent Japanese language ability.
Authorized to work in Japan.
【FOR FURTHER INFORMATION】
Contact Jessica Sanusi:
email@example.com // 050-1751-6021
Click “Apply now” in the top right.